Abstract
The detection of antibodies against aquaporin-4 (AQP4) has improved the diagnosis of neuromyelitis optica (NMO). We evaluated a recently established cell-based anti-AQP4 assay in 273 patients with inflammatory CNS demyelination. The assay had a specificity of 99% and a sensitivity of 56% to detect all NMO patients and of 74% to detect the recurrent NMO patients, similar to the initial studies reported. AQP4 antibodies were absent in monophasic NMO patients, while samples in recurrent cases remained positive during follow-up. We conclude that the pathogenesis of monophasic NMO may be different from that of relapsing NMO.
Original language | English |
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Pages (from-to) | 1527-30 |
Number of pages | 4 |
Journal | Multiple Sclerosis Journal |
Volume | 17 |
Issue number | 12 |
DOIs | |
Publication status | Published - Dec 2011 |
Externally published | Yes |
Keywords
- Aquaporin 4/immunology
- Autoantibodies/blood
- Diagnosis, Differential
- Fluorescent Antibody Technique, Indirect
- Follow-Up Studies
- Humans
- Immunoglobulin G/blood
- Multiple Sclerosis/diagnosis
- Neuromyelitis Optica/diagnosis
- Recurrence
- Sensitivity and Specificity